- Research article
- Open Access
ITS2 data corroborate a monophyletic chlorophycean DO-group (Sphaeropleales)
- Alexander Keller†1,
- Tina Schleicher†1,
- Frank Förster1,
- Benjamin Ruderisch1,
- Thomas Dandekar1,
- Tobias Müller1 and
- Matthias Wolf1Email author
© Keller et al; licensee BioMed Central Ltd. 2008
- Received: 12 March 2008
- Accepted: 25 July 2008
- Published: 25 July 2008
Within Chlorophyceae the ITS2 secondary structure shows an unbranched helix I, except for the 'Hydrodictyon' and the 'Scenedesmus' clade having a ramified first helix. The latter two are classified within the Sphaeropleales, characterised by directly opposed basal bodies in their flagellar apparatuses (DO-group). Previous studies could not resolve the taxonomic position of the 'Sphaeroplea' clade within the Chlorophyceae without ambiguity and two pivotal questions remain open: (1) Is the DO-group monophyletic and (2) is a branched helix I an apomorphic feature of the DO-group? In the present study we analysed the secondary structure of three newly obtained ITS2 sequences classified within the 'Sphaeroplea' clade and resolved sphaeroplealean relationships by applying different phylogenetic approaches based on a combined sequence-structure alignment.
The newly obtained ITS2 sequences of Ankyra judayi, Atractomorpha porcata and Sphaeroplea annulina of the 'Sphaeroplea' clade do not show any branching in the secondary structure of their helix I. All applied phylogenetic methods highly support the 'Sphaeroplea' clade as a sister group to the 'core Sphaeropleales'. Thus, the DO-group is monophyletic. Furthermore, based on characteristics in the sequence-structure alignment one is able to distinguish distinct lineages within the green algae.
In green algae, a branched helix I in the secondary structure of the ITS2 evolves past the 'Sphaeroplea' clade. A branched helix I is an apomorph characteristic within the monophyletic DO-group. Our results corroborate the fundamental relevance of including the secondary structure in sequence analysis and phylogenetics.
- Secondary Structure
- Secondary Structure Information
- Compensatory Base Change
- Apomorphic Feature
- Autapomorphic Feature
Taxonomists face inconsistent or even contradictory clues when they examine the affiliation of organisms to higher taxonomic groupings. Several characters may yield alternative hypotheses explaining their evolutionary background. This also applies to the taxonomic position of the Sphaeropleaceae [1–23]. Different authors affiliate the green algal family by morphological characters to either ulvophytes or chlorophytes, until amendatory Deason et al.  suggested that the Neochloridaceae, the Hydrodictyaceae and the Sphaeropleaceae should be grouped as Sphaeropleales within the chlorophytes, since all of them have motile biflagellate zoospores with a direct-opposite (DO) confirmation of basal bodies.
Subsequently, other taxonomic lineages (the 'Ankistrodesmus' clade, the 'Bracteacoccus' clade, the 'Pseudomuriella' clade, Pseudoschroederia, the 'Scenedesmus' clade, Schroederia and the 'Zofingiensis' clade) were added to this biflagellate DO group, because they show molecular affiliation to either Neochloridaceae or Hydrodictyaceae .
Although nowadays most authors agree that the DO group is monophyletic, until now no study pinpointed the taxonomic linkage of the name-giving 'Sphaeroplea' clade to the remaining 'core Sphaeropleales' persuasively with genetic evidence [6, 23], i.e. the sister clade remains unclear [15, 24]. Likewise, with respect to morphology, studies of 18S and 26S rRNA gene sequences neither resolve the basal branching patterns within the Chlorophyceae with high statistical power nor corroborate a monophyletic biflagellate DO group without ambiguity [6, 23].
Müller et al.  obtained moderate statistical support for the close relationship of the 'Sphaeroplea' clade and the 'core Sphaeropleales' with profile distances of 18S and 26S rDNA. In this study we followed and expanded their methodology with a very different phylogenetic marker. The internal transcribed spacer 2 (ITS2), the region of ribosomal RNA between the 5.8S rRNA gene and the large subunit (26S rDNA) has proven to be an appropriate marker for the study of small scale phylogenies of close relatives [26–29]. The sequence is in contrast to the bordering regions of ribosomal subunits evolutionary not conserved, thus genetic differentiation is detectable even in closely related groups of organisms. By contrast, the secondary structure seems to be well conserved and thus provides clues for higher taxonomic studies [27, 30–33]. Secondary structure information is furthermore especially interesting within the Chlorophyceae, because van Hannen et al.  described an uncommon branching of ITS2 helix 1 within the genera Desmodesmus, Hydrodictyon  and Scenedesmus. It is not known when this feature evolved and whether it is, as we expect, an apomorphic feature for the DO-group. It is obvious that phylogenetic statements should be improvable by inclusion of structural information in common sequence analysis. For example, Grajales et al.  calculated morphometric matrices from ITS2 secondary structures for phylogenetic analyses, but treated information of sequence and structure as different markers. Here we combine sequence with structural information in just one analysis. Aside from the biological problem, we address the pivotal question of a methodological pipeline for sequence-structure phylogenetics using rDNA data.
DNA extraction, amplification and sequencing
Extraction of genomic DNA from cultured cells of Ankyra judayi, Atractomorpha porcata and Sphaeroplea annulina was done using Dynabeads® (DNA DIRECT Universal, Dynal Biotech, Oslo, Norway) according to the manufacturer's protocol. PCR reactions were performed in a 50 μl reaction volume containing 25 μl FastStart PCR Master (Roche Applied Science), 5 μl gDNA and 300 nM of the primers ITS3 (5'-GCA TCG ATG AAG AAC GCA GC-3') and ITS4 (5'-TCC TCC GCT TAT TGA TAT GC-3') designed by White et al. .
Cycling conditions for amplification consisted of 94°C for 10 min, 30 cycles of 94°C for 30 s, 50°C for 30 s and 72°C for 45 s, followed by a final extension step of 10 min at 72°C. PCR products were analysed by 3% agarose gel electrophoresis and ethidium bromide staining.
PCR probes where purified with the PCR Purificaton Kit (Qiagen) and where quantified by spectrometry. Each sequencing probe was prepared in an 8 μl volume containing 20 ng DNA and 1.25 μM Primer. Sequencing was carried out using an annealing temperature of 50°C with the sequencer Applied Biosystems QST 3130 Genetic Analyzer by the Institute of Hygiene and Microbiology (Würzburg, Germany).
ITS2 secondary structure prediction
Chlorophyte species used for this investigation.
Ankyra judayi (G.M. Smith) Fott 1957
Atractomorpha porcata Hoffman 1984 strain
Sphaeroplea annulina (Roth) C. Agardh 1824
Sphaeroplea annulina (Roth) C. Agardh 1824
Haematococcus droebakensis Wollenweber 1908
Dunaliella parva Lerche 1937
Dunaliella salina (Dunal) Teodoresco 1905
Hydrodictyon africanum Yamanouchi 1913
Hydrodictyon patenaeforme Pocock
Hydrodictyon reticulatum (Linnaeus) B. de St.-Vincent 1824
Pediastrum braunii Wartmann 1862
Pediastrum duplex Meyen 1829
Pseudopediastrum boryanum (Raciborski) Sulek 1969
Sorastrum spinulosum Nägeli 1849
Stauridium tetras (Ehrenberg) Ralfs 1844
EL 0207 CT
Bulbochaete hiloensis (Nordstedt) Tiffany 1937
Oedogonium cardiacum (Hassall) Wittrock 1870
Oedogonium nodulosum Wittrock 1872
Oedogonium oblongum Wittrock 1872
Oedogonium undulatum (Brébisson) A. Braun 1854
Chlamydomonas incerta Pascher 1927
Chlamydomonas komma Skuja 1934
Chlamydomonas petasus Ettl
Chlamydomonas reinhardtii Dangeard 1888
Chlamydomonas typica Deason & Bold 1960
Eudorina elegans Ehrenberg 1831
Eudorina unicocca G.M. Smith 1930
Gonium octonarium Pocock 1955
Gonium pectorale O.F. Müller 1773
Gonium quadratum E. G. Pringsheim ex H. Nozaki
Pandorina morum (O.F. Müller) Bory de Saint-Vincent 1824
Volvox dissipatrix (Shaw) Printz
Volvox rousseletii G.S.West
Volvulina steinii Playfair 1915
Yamagishiella unicocca (Rayburn & Starr) Nozaki 1992
Desmodesmus abundans (Kirchner) Hegewald 2000
Desmodesmus bicellularis (Chodat) An, Friedl & Heg. 1999
Desmodesmus communis (Hegewald) Hegewald 2000
Desmodesmus elegans (Hortobágyi) Heg. & Van. 2007
Desmodesmus opoliensis (P.G. Richter) Hegewald 2000
Desmodesmus pleiomorphus (Hindák) Hegewald 2000
Desmodesmus quadricauda (Turpin) Hegewald
Scenedesmus acuminatus (Lagerheim) Chodat 1902
Scenedesmus acutiformis (B. Schröder) F. Hindák 1990
Scenedesmus basiliensis Chodat 1926
Scenedesmus dimorphus (Turpin) Kützing 1833
Scenedesmus longus Meyen 1829 ex Ralfs
Scenedesmus obliquus (Turpin) Kützing 1833
Scenedesmus pectinatus Meyen 1828
Scenedesmus platydiscus (G.M. Smith) Chodat 1926
Scenedesmus raciborskii Woloszynska 1914
Scenedesmus regularis Svirenko
Scenedesmus wisconsinensis (G.M. Smith) Chodat 1996
Alignment and phylogenetic analyses
Using 4SALE [40, 41] with its ITS2 specific scoring matrix, we automatically aligned sequences and structures simultaneously. Sequence-structure alignment is available at the ITS2 database supplements page. For the complete alignment we tested for appropriate models of nucleotide substitution using the Akaike Information Criterion (AIC) as implemented in Modeltest . The following PAUPblock was used for all maximum likelihood based phylogenetic analyses with PAUP* : Lset Base = (0.2299 0.2415 0.2152) Nst = 6 Rmat = (1.4547 3.9906 2.0143 0.1995 3.9906) Rates = gamma Shape = 1.1102 Pinvar = 0.0931;. A maximum likelihood (ML) analysis was performed with a heuristic search (ten random taxon addition replicates) and nearest neighbour interchange (NNI) .
Maximum parsimony (MP)  was accomplished with gaps treated as missing data and all characters coded as "unordered" and equally weighted. Additionally, we clustered taxonomic units with neighbour-joining (NJ)  using maximum likelihood distances. Furthermore, with MrBayes  a Bayesian analysis (B) was carried out for tree reconstruction using a general time reversible substitution model (GTR) [48–50] with substitution rates estimated by MrBayes (nst = 6). Moreover, using ProfDist, a profile neighbour-joining (PNJ) tree [51, 25] was calculated using the ITS2 specific substitution model available from the ITS2 Database. PNJ was also performed with predefined profiles (prePNJ) of all the clades given in Table 1.
New ITS2 sequences
ITS2 sequence and secondary structure information
ITS2 sequence lengths of all studied species ran from 202 to 262 nucleotides (nt), 235 nt on average. The GC contents of ITS2 sequences ranged from 36.84% to 59.92%, with a mean value of 52.42%. The number of base pairs (bp) varied between 64 and 89 bp and averaged 77 bp. The cropped alignment (50% structural consensus) showed that 23% of the nucleotides had at least a 50% consistency in their pairings. Compensatory base changes (CBCs) as well as hemi-CBCs (all against all) range from 0 to 16 with a mean of 6.6 CBCs (Fig. 2). Sequence pairs lacking CBCs were exclusively found within the same major clade.
Characteristics in a conserved part of alignment
In agreement with Coleman , the 5' side part near the tip of helix III was highly conserved including the UGGU motif [54, 55, 30], likewise the UGGGU motif in case of Chlorophyceae. We selected a part of the alignment at this position with adjacent columns (Fig. 2) to verify the suggested conservation. Having a closer look at this part of helix III, in our case, it showed typical sequence and structural characteristics for distinct groups. Studied species of the 'Oedogonium' clade possess at position 3 in the selected part of the alignment an adenine and in addition at positions 3–5 paired bases. In contrast, the CW-group solely possessed three consecutively paired bases in this block, but not the adenine. A typical pattern for clades of the DO-group was a twofold motif of 3 bases: uracile, adenine and guanine at positions 7–9, which is repeated at positions 11–13. This could be a duplication, which results in a modified secondary structure. In addition, the 'core Sphaeropleales' ('Hydrodictyon' clade and 'Scenedesmus' clade) showed an adenine base change at position 6, compared to all other clades.
Phylogenetic tree information
The PAUP* calculation applying maximum Parsimony included a total of 479 characters, whereas 181 characters were constant, 214 variable characters were parsimony-informative compared to 84 parsimony-uninformative ones.
Bootstrap support values for basal branches of all methods applied.
The 'Hydrodictyon' clade, the 'Scenedesmus' clade and the 'Sphaeroplea' clade form one cluster that was strongly supported by high bootstrap values of 67–96% (node "g"). The three clades composed the DO-group. The opposite cluster included the 'Dunaliella' and the 'Reinhardtii' clade, forming the CW-group. The 'Oedogonium' clade was chosen as the outgroup . Both clusters (CW-group and 'Oedogonium' clade) were strongly supported by bootstrap values of 84–100% (nodes "i" and "h").
Except for the Bayesian analysis (least support for node "c"), all applied methods yielded node "e" as the weakest point within the basal (labelled) branches (Table 2), which presents the relationship between the 'Hydrodictyon' and the 'Scenedesmus' clade on the one hand and the 'Dunaliella', the 'Oedogonium', the 'Reinhardtii' and the 'Sphaeroplea' clade on the other hand. The phylogenetic tree resulting from neighbour-joining analysis by PAUP* (Fig. 3) did not support node "e" at all, but strongly supported the remaining labelled branches. The maximum likelihood analysis by PAUP* (Fig. 4) did not encourage node "e" either. Both maximum likelihood methods did not even support nodes "a" ('true Scenedesmus' compared to remaining clades) and "c" ('Scenedesmus' opposite to remaining clades). All other basal branches were supported by this method.
Varying neighbour-joining analyses by ProfDist (NJ, PNJ, prePNJ, strPNJ) supported all basal branches – except for the weakest node "e" (average support) – with very high bootstrap support values of 84–100%. The maximum Parsimony method gave average support (63 and 62%) for node "c" and "e" and high bootstrap values (80–100%) for the remaining basal clades. The Bayesian analysis offered posterior probabilities of 0.72 for node "c" and 0.86–1.0 for the remaining basal nodes. For further sister group relations see Fig. 3 and 4.
In comparison, the topology of the phylogenetic tree based on the 50% cropped alignment did not change, but the bootstrap support values were lower in all cases (data not shown).
Using three newly obtained ITS2 sequences from Ankyra judayi, Atractomorpha porcata and Sphaeroplea annulina (Sphaeropleaceae) in this study we aimed to pursue two consecutive questions concerning the phylogenetic relationships within Chlorophyceae. (1) What is the phylogenetic position of the newly sequenced algae relative to the 'core Sphaeropleales' and could the biflagellate DO-group be regarded as monophyletic? (2) How does the secondary structure of the new ITS2 sequences look like and is an autapomorphic feature of the secondary structure associated with the monophyletic DO-group?
Considering the question (1) Buchheim et al.  and Wolf et al.  approached the problem with 18S + 26S rDNA and 18S rDNA data, but the relationship between the 'core Sphaeropleales' and the Sphaeropleaceae remained unclear. However, in their studies, Ankyra, Atractomorpha and Sphaeroplea clustered in a monophyletic clade named Sphaeropleaceae. We confirm this 'Sphaeroplea' clade with all three genera being strongly separated from other clades. As a result of a Bayesian analysis on a combined 18S and 26S rDNA dataset Shoup and Lewis  also found the Sphaeropleaceae as the most basal clade within the Sphaeropleales, but again the analysis lacked a strong backing. Beside these difficulties the 'core Sphaeropleales' were already shown to be monophyletic with high certainty [6, 25, 62, 61, 23].
The DO-group (Sphaeropleales including the 'Sphaeroplea' clade) as emended by Deason et al. , for which the directly opposed basal body orientation and basal body connection features are verified [63–65], is now strongly supported by molecular phylogenetic analyses. There was already evidence of an extended DO-group [6, 66, 67], however, for some groups ultrastructural results are still lacking, and even though the collective basal body orientation and connection imply a monophyletic DO-group, until now no molecular phylogenetic analysis could show this with solid support [6, 62, 24, 23]. We demonstrate for the first time with robust support values for the equivocal nodes that the 'core Sphaeropleales', the 'Sphaeroplea' clade, and the Sphaeropleales are monophyletic.
Regarding question (2), for all structures of the 'Hydrodictyon' and the 'Scenedesmus' clade, helix I shows the typical branching (Y-structure). Initially, An et al.  proposed a secondary structure model with an unbranched helix I for ITS2 sequences of 'Scenedesmus' clade members. Thereafter, van Hannen et al.  updated the model by folding the nucleotide sequences based upon minimum free energy and found a branched helix I as the most energetically stable option. The branching is result of an insertion of approximately 25 nucleotides capable of folding as an individual stem within the 5' end of the first helix. However, ITS2 sequence and secondary structure information of further 'core Sphaeropleales' members, e.g. the 'Ankistrodesmus' clade and the 'Bracteacoccus' clade, lacks hitherto. In contrast, the Y-structure is absent within the 'Sphaeroplea' clade and any other investigated group so far. Thus this feature is – contrary to our expectation – not an autapomorphic character for the biflagellate DO-group as a whole but for the 'core Sphaeropleales'.
Regarding future work, the resolution among the main clades of Chlorophyceae was statistically poorly supported in previous studies [68, 15, 6, 23]. Pröschold and Leliaert  reviewed the systematics of green algae by applying a polyphasic approach, but did not yield a clear resolution regarding a sister taxon to the Sphaeropleales. Since they are not yet available, ITS2 sequences of chaetopeltidalean and chaetophoralean taxa could not be included in the present study and therefore the phylogenetic relationships between the main Chlorophyceae clades remain open. We recommend involving sequence and secondary structure information of chaetopeltidalean and chaetophoralean ITS2 sequences in future studies to find out if the monophyletic biflagellate DO-group could be further extended to a general monophyletic DO-group containing quadri- and biflagellate taxa. A genome-wide approach indicates that Sphaeropleales and Chlamydomonadales are sister taxa, however only a few organisms are included in this study . An additional uprising question is when the Y has evolved within the 'core Sphaeropleales'. This could be resolved by inclusion of other members (e.g. Bracteacoccus) in further studies.
The two major reasons contributing to the robust results presented here are the change of the phylogenetic marker and the inclusion of secondary structure information. In contrast to previous phylogenetic work concerning Chlorophyceae, this study is based on the ITS2, which offers a resolution power for relationships from the level of subspecies up to the order level, because of their variable sequence but conserved secondary structure [26, 30–33]. Hitherto commonly used markers in contrast are a lot more restricted. Using 4SALE  with implemented structure consideration, we could achieve for the first time a global simultaneously generated sequence-structure alignment (c.f. Fig. 1) yielding specific sequence and structural features distinguishing different algae lineages (c.f. Fig. 2).
In summary, the powerful combination of the ITS2 rRNA gene marker plus a multiple global alignment based synchronously on sequence and secondary structure yielded high bootstrap support values for almost all nodes of the computed phylogenetic trees. Thus, the relationship of Sphaeropleaceae is here resolved, being a part of the Sphaeropleales representing the monophyletic biflagellate DO-group. Furthermore, we could elucidate a branched helix I of ITS2 as an autapomorphic feature within the DO-group. This feature could be found only in the 'Hydrodictyon' and the 'Scenedesmus' clade. Our results corroborate the presented methodological pipeline, the fundamental relevance of secondary structure consideration, as well as the elevated power and suitability of ITS2 in phylogenetics. For a methodological improvement it is suitable to ameliorate the alignment algorithm in further considering horizontal dependencies of paired nucleotides, and moreover in future ITS2 studies it is suggested to include sequence and secondary structure information of hitherto not regarded taxa to resolve the chlorophycean phylogeny.
Financial support for AK and TS was provided by the Deutsche Forschungsgemeinschaft (DFG) grant (Mu-2831/1-1). AK was additionally supported by BIGSS (Elite graduate school). FF was supported by the Bundesministerium für Bildung und Forschung (BMBF) grant FUNCRYPTA. The newly obtained sequences originate from SAG cultures (Göttingen, Germany). We thank the Institute of Hygiene and Microbiology (Würzburg, Germany) for sequencing. We thank T. Ulmar Grafe (University of Brunei Darussalam) for proof-reading English.
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